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Results: 1-19 |
Results: 19
COMPROMISED FATTY-ACID OXIDATION IN MITOCHONDRIAL DISORDERS
Authors: HAGENFELDT L
Citation: L. Hagenfeldt, COMPROMISED FATTY-ACID OXIDATION IN MITOCHONDRIAL DISORDERS, Journal of inherited metabolic disease, 21(5), 1998, pp. 613-617
FATTY-ACID OXIDATION IN FIBROBLASTS FROM PATIENTS WITH DEFECTS IN BETA-OXIDATION AND IN THE RESPIRATORY-CHAIN
Authors: VENIZELOS N VONDOBELN U HAGENFELDT L
Citation: N. Venizelos et al., FATTY-ACID OXIDATION IN FIBROBLASTS FROM PATIENTS WITH DEFECTS IN BETA-OXIDATION AND IN THE RESPIRATORY-CHAIN, Journal of inherited metabolic disease, 21(4), 1998, pp. 409-415
BENEFITS OF NEONATAL SCREENING FOR CONGENITAL ADRENAL-HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) IN SWEDEN
Authors: THILEN A NORDENSTROM A HAGENFELDT L VONDOBELN U GUTHENBERG C LARSSON A
Citation: A. Thilen et al., BENEFITS OF NEONATAL SCREENING FOR CONGENITAL ADRENAL-HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) IN SWEDEN, Pediatrics, 101(4), 1998, pp. 111-115
A METHYLENETETRAHYDROFOLATE REDUCTASE GENE POLYMORPHISM IN ISCHEMIC STROKE AND IN CAROTID-ARTERY STENOSIS
Authors: KOSTULAS K CRISBY M HUANG WX LANNFELT L HAGENFELDT L EGGERTSEN G KOSTULAS V HILLERT J
Citation: K. Kostulas et al., A METHYLENETETRAHYDROFOLATE REDUCTASE GENE POLYMORPHISM IN ISCHEMIC STROKE AND IN CAROTID-ARTERY STENOSIS, European journal of clinical investigation, 28(4), 1998, pp. 285-289
TREATMENT OF ADRENOLEUKODYSTROPHY WITH BONE-MARROW TRANSPLANTATION
Authors: MALM G RINGDEN O ANVRET W VONDOBELN U HAGENFELDT L ISBERG B KNUUTILA S NENNESMO I WINIARSKI J MARCUS C
Citation: G. Malm et al., TREATMENT OF ADRENOLEUKODYSTROPHY WITH BONE-MARROW TRANSPLANTATION, Brain pathology, 7(4), 1997, pp. 1348-1348
TREATMENT OF ADRENOLEUKODYSTROPHY WITH BONE-MARROW TRANSPLANTATION
Authors: MALM G RINGDEN O ANVRET M VONDOBELN U HAGENFELDT L ISBERG B KNUUTILA S NENNESMO I WINIARSKI J MARCUS C
Citation: G. Malm et al., TREATMENT OF ADRENOLEUKODYSTROPHY WITH BONE-MARROW TRANSPLANTATION, Acta paediatrica, 86(5), 1997, pp. 484-492
TYROSINE TRANSPORT IN SCHIZOPHRENIA
Authors: WIESEL FA ANDERSSON J WIESELGREN IM BLOMQVIST G BJERKENSTEDT L HAGENFELDT L
Citation: Fa. Wiesel et al., TYROSINE TRANSPORT IN SCHIZOPHRENIA, Schizophrenia research, 18(2-3), 1996, p.
REDUCED TYROSINE TRANSPORT IN SCHIZOPHRENIA
Authors: BJERKENSTEDT L WIESEL FA HAGENFELDT L
Citation: L. Bjerkenstedt et al., REDUCED TYROSINE TRANSPORT IN SCHIZOPHRENIA, Schizophrenia research, 18(2-3), 1996, p.
VIGABATRIN THERAPY IN 6 PATIENTS WITH SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY
Authors: GIBSON KM JAKOBS C OGIER H HAGENFELDT L EEGOLOFSSON KE EEGOLOFSSON O AKSU F WEBER HP ROSSIER E VOLLMER B LEHNERT W
Citation: Km. Gibson et al., VIGABATRIN THERAPY IN 6 PATIENTS WITH SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY, Journal of inherited metabolic disease, 18(2), 1995, pp. 143-146
CLINICAL AND BIOCHEMICAL PRESENTATION OF LONG-CHAIN 3-HYDROXYACYL-COADEHYDROGENASE-DEFICIENCY
Authors: HAGENFELDT L VENIZELOS N VONDOBELN U
Citation: L. Hagenfeldt et al., CLINICAL AND BIOCHEMICAL PRESENTATION OF LONG-CHAIN 3-HYDROXYACYL-COADEHYDROGENASE-DEFICIENCY, Journal of inherited metabolic disease, 18(2), 1995, pp. 245-248
TYROSINE TRANSPORT IN SCHIZOPHRENIA
Authors: WIESEL FA VENIZELOS N BJERKENSTEDT L HAGENFELDT L
Citation: Fa. Wiesel et al., TYROSINE TRANSPORT IN SCHIZOPHRENIA, Schizophrenia research, 13(3), 1994, pp. 255-258
CREATINE TREATMENT IN MELAS
Authors: HAGENFELDT L VONDOBELN U SOLDERS G KAIJSER L
Citation: L. Hagenfeldt et al., CREATINE TREATMENT IN MELAS, Muscle & nerve, 17(10), 1994, pp. 1236-1237
LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE IN CHORIONIC VILLI, FETAL LIVER AND FIBROBLASTS AND PRENATAL-DIAGNOSIS OF 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY
Authors: VONDOBELN U VENIZELOS N WESTGREN M HAGENFELDT L
Citation: U. Vondobeln et al., LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE IN CHORIONIC VILLI, FETAL LIVER AND FIBROBLASTS AND PRENATAL-DIAGNOSIS OF 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY, Journal of inherited metabolic disease, 17(2), 1994, pp. 185-188
SEVERITY OF MUTATION IN THE PHENYLALANINE-HYDROXYLASE GENE INFLUENCESPHENYLALANINE METABOLISM IN PHENYLKETONURIA AND HYPERPHENYLALANINEMIAHETEROZYGOTES
Authors: SVENSSON E ISELIUS L HAGENFELDT L
Citation: E. Svensson et al., SEVERITY OF MUTATION IN THE PHENYLALANINE-HYDROXYLASE GENE INFLUENCESPHENYLALANINE METABOLISM IN PHENYLKETONURIA AND HYPERPHENYLALANINEMIAHETEROZYGOTES, Journal of inherited metabolic disease, 17(2), 1994, pp. 215-222
THYMINE-URACILURIA - A DISEASE OR A FORTUITOUS FINDING
Authors: HAVERKORN C BLOMQUIST HK SNELLMAN K AHLMAN H VONDOBELN U HAGENFELDT L
Citation: C. Haverkorn et al., THYMINE-URACILURIA - A DISEASE OR A FORTUITOUS FINDING, Pediatric research, 36(1), 1994, pp. 10000018-10000018
BETA-OXIDATION ENZYMES IN FIBROBLASTS FROM PATIENTS WITH 3-HYDROXYDICARBOXYLIC ACIDURIA
Authors: VENIZELOS N IJLST L WANDERS RJA HAGENFELDT L
Citation: N. Venizelos et al., BETA-OXIDATION ENZYMES IN FIBROBLASTS FROM PATIENTS WITH 3-HYDROXYDICARBOXYLIC ACIDURIA, Pediatric research, 36(1), 1994, pp. 111-114
THE MODIFYING INFLUENCE OF ANESTHESIA ON POSTOPERATIVE PROTEIN CATABOLISM
Authors: GIESECKE K KLINGSTEDT C LJUNGQVIST O HAGENFELDT L
Citation: K. Giesecke et al., THE MODIFYING INFLUENCE OF ANESTHESIA ON POSTOPERATIVE PROTEIN CATABOLISM, British Journal of Anaesthesia, 72(6), 1994, pp. 697-699
ESTABLISHMENT OF A TISSUE-BANK FOR FETAL STEM-CELL TRANSPLANTATION
Authors: WESTGREN M EK S BUI TH HAGENFELDT L MARKLING L PSCHERA H SEIGER A SUNDSTROM E RINGDEN O
Citation: M. Westgren et al., ESTABLISHMENT OF A TISSUE-BANK FOR FETAL STEM-CELL TRANSPLANTATION, Acta obstetricia et gynecologica Scandinavica, 73(5), 1994, pp. 385-388
FATAL NEONATAL LACTIC-ACIDOSIS WITH RESPIRATORY INSUFFICIENCY DUE TO COMPLEX-I AND COMPLEX-IV DEFICIENCY
Authors: VONDOBELN U WIBOM R AHLMAN H NENNESMO I NYCTELIUS H HULTMAN E HAGENFELDT L
Citation: U. Vondobeln et al., FATAL NEONATAL LACTIC-ACIDOSIS WITH RESPIRATORY INSUFFICIENCY DUE TO COMPLEX-I AND COMPLEX-IV DEFICIENCY, Acta paediatrica, 82(12), 1993, pp. 1079-1081
Risultati: 1-19 |